Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs12121543
MTHFR
0.851 0.240 1 11794614 intron variant C/A snv 0.21 4
rs13306556
MTHFR
1 11792053 intron variant C/T snv 0.10 2
rs6541006
MTHFR
1 11797469 intron variant A/G;T snv 2
rs17037388
MTHFR
1 11797979 intron variant A/G snv 0.17 1
rs17375901
MTHFR
1.000 0.080 1 11792459 intron variant C/T snv 4.6E-02 1
rs17421511
MTHFR
1.000 0.040 1 11797731 intron variant G/A snv 0.13 1
rs3737964
MTHFR ; CLCN6
1.000 0.080 1 11806987 intron variant T/A;C;G snv 1
rs3818762
MTHFR
1 11790946 intron variant G/C snv 0.26; 1.7E-03 0.23 1
rs45553335
MTHFR
1 11798900 intron variant T/C snv 0.14 1
rs4846052
MTHFR
1.000 0.080 1 11797894 intron variant T/A;C snv 1
rs576853093
MTHFR
1 11790946 intron variant -/C;CACACACACACAC ins 6.2E-03 1
rs777661576
MTHFR
1.000 1 11790916 intron variant C/T snv 4.0E-06; 8.0E-06 1.4E-05 1
rs786204030
MTHFR
0.882 0.080 1 11791276 stop gained C/T snv 3
rs121434294
MTHFR
1.000 1 11800251 stop gained G/A snv 1
rs377443637
MTHFR
1.000 1 11794823 stop gained G/A snv 1.2E-05 7.0E-06 1
rs763539350
MTHFR
1.000 1 11802915 stop gained G/A;C snv 8.0E-06; 4.0E-05 1
rs786204007
MTHFR
1.000 1 11802941 stop gained C/G;T snv 4.0E-06 1
rs786204035
MTHFR
1.000 1 11790853 stop gained CA/AC mnv 1
rs986604359
MTHFR
1.000 1 11802963 stop gained G/A snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174